Pharmaceutical administration of adenosine agonists

ABSTRACT

The present invention relates to a method of inducing proliferation of bone marrow cells in a subject, compromising administering to the subject an effective amount of an adenosine A1 receptor agonist. The present invention further relates to a method for preventing reduction in level of leukocytes in a subject as a result of a treatment comprising administering to the individual an effective amount of an adenosine A1 receptor agonist. In addition, the invention relates to a method of treatment of an individual comprising administering to the subject a therapeutic drug in combination with an adenosine A1 receptor agonist.

This application is a continuation-in-part of application Ser. No. 09/700,744 filed on Jan. 9, 2001, which is the national phase under 35 USC §371 of PCT International Application No. PCT/IL00/00014 which has an International filing date of Jan. 7, 2000, which designated the United States, of America the entire contents of which are hereby incorporated by reference.

FIELD OF THE INVENTION

This invention relates to drugs for use in cancer therapy. More specifically, the present invention concerns drugs which induce proliferation of cells of the hematopoietic system.

1. Prior Art

The following is a list of prior art references considered to be relevant as background to the invention:

1. Daly, J. W., Adenosine receptors: Targets for future drugs. J. Med. Chem., 25:197-207, 1982.

2. Stiles, G. L., Adenosine receptors and beyond: Molecular mechanisms of physiological regulation, Clin. Res., 38:10-18, 1990.

3. Collis, M. G., The vasodilator role of adenosine, Pharmacol. Ther, 41:143-162, 1989.

4. Fishman et al., Extracellular adenosine acts as a chemoprotective agent, Proceeding of the American Association for Cancer Research, 39:470, 1998.

5. Moos, W. H., et al., N⁶-cycloalkyladenosines. Potent A₁ selective adenosine agonists, J. Medicinal Chemistry 28:1383-1384, 1985.

6. Jacobson, K. A et al., Functionalized congeners of adenosine, J. Medicinal Chemistry 28:1341-1346, 1985.

7. U.S. Pat. No. 5,998,387.

8. U.S. Pat. No. 5,998,388

9. U.S. Pat. No. 5,498,605.

10. U.S. Pat. No. 4,791,103.

2. Background of the Invention

Adenosine is an extracellular messenger generated by all cells in the body. It is known to regulate different physiological processes within cells through binding to specific cell surface receptors—A₁ and A₂ receptors ^((1,2,3)). It was recently demonstrated that adenosine inhibits proliferation of tumor cells and induces proliferation of bone marrow cells ⁽⁴⁾. Further more it was also shown that adenosine can protect white blood cells, particularly neutrophils, from destruction which is otherwise caused by chemotherapeutic drugs ⁽⁴⁾.

SUMMARY OF THE INVENTION

The present invention is based on the surprising findings that (i) the effect of adenosine in inducing proliferation of bone marrow cells can be inhibited by A₁ receptor antagonists (antagonist that inhibits binding of adenosine to adenosine A₁ receptor), and (ii) the effect of adenosine can be mimicked by an adenosine A₁ receptor agonist (“A₁RAg”). These findings led to the conclusion that the bone marrow proliferation-induction effect of adenosine is mediated, at least to some extent through the A₁ receptor, and that accordingly A₁RAg may be used to induce proliferation of bone marrow cells, in a wide variety of clinical situations where such proliferation is therapeutically beneficial.

The present invention provides, by a first of its aspects, a pharmaceutical composition for use in inducing proliferation of bone marrow cells, comprising a pharmaceutically acceptable carrier, excipient or diluent and, as an active ingredient, an effective amount of an A₁RAg.

The present invention provides, by a second of its aspects, use of an A₁RAg for the production of a pharmaceutical composition for use in inducing proliferation of bone marrow cells.

The present invention further provides a method of inducing proliferation of bone marrow cells in a subject, comprising administering to the subject an effective amount of an A₁RAg.

The term “effective amount” used above and below should be understood as meaning an amount of an A₁RAg which is capable of achieving a desired therapeutic effect, particularly, in inducing proliferation of bone marrow cells. The desired therapeutic effect depends on the type and mode of treatment. When, for example, said A₁RAg is administered to counter drug-induced leukopenia, an effective amount thereof may be an amount which protects the treated subject against the drug-induced reduction in the count of leukocytes, particularly neutrophils; an amount of the active ingredient which can give rise to an increase in an already decreased level of such cells, e.g. restore the level to a normal level or sometimes even above; etc. The man of the art will have no difficulties, on the basis of a limited number of routine experiments, to determine an effective amount in each case.

As will be appreciated, the effective amount may also depend on the treated subject's gender, on the individual's weight, on the therapeutic regime, namely whether the A₁RAg is administered once daily, several times daily, once in several days, etc. Furthermore, the effective amount may depend on the exact nature or etiology of the disease or condition which is being treated or intended to be prevented.

According to one embodiment of the invention, the A₁RAg are adenosine derivatives carrying at least an N⁶-substituent. Other positions may also be substituted. In fact, it has been found that the biological activity of an adenosine derivative may be enhanced by modifying other parts of the nucleotide, for example, at the 2- and/or 5′-positions (e.g. with chloro atoms). Such substituents were found to increase the molecule's A₁ selectivity.

The adenosine derivatives which can be used according to the present invention are generally defined by the following formula (I):

wherein

R₁ represents a lower alkyl, cycloalkyl, preferably C₃-C₈ cycloalkyl (including the well known cyclohexyl and cyclopentyl containing derivatives, recognized as CPA and CHA, respectively), the cycloalkyl group may be substituted with, for example, a hydroxyl or lower alkyl; R₁ also represents a hydroxyl or hydroxyalkyl; a phenyl anilide, or lower alkyl phenyl, all optionally substituted by one or more substituents, for example, halogen, lower alkyl, haloalkyl such as trifluoromethyl, nitro, cyano, —(CH₂)_(m)CO₂R^(a), —(CH₂)_(m)CONR₂R⁴R^(b), —(CH₂)_(m)COR^(a), m representing an integer from 0 to 6; —SOR^(c), —SO₂R^(c), —SO₃H, —SO₂NR^(a)R^(b), —OR^(a), —SR^(a), —NHSO₂R^(c), —NHCOR^(a), —NR^(a)R^(b) or —NHR^(a)CO₂R^(b); wherein

R^(a) and R^(b) represent independently a hydrogen, lower alkyl, alkanoyl, phenyl or naphthyl (the latter may be partially saturated) the alkyl group optionally being substituted with a substituted or unsubstituted phenyl or phenoxy group; or when R₁ represents —NR^(a)R^(b), said R^(a) and R^(b) form together with the nitrogen atom a 5- or 6- membered heterocyclic ring optionally containing a second heteroatom selected from oxygen or nitrogen, which second nitrogen heteroatom may optionally be further substituted by hydrogen or lower alkyl; or —NR^(a)R^(b) is a group of general formulae (II) or (III):

 wherein

n is an integer from 1 to 4;

Z is hydrogen, lower alkyl or hydroxyl;

Y is hydrogen, lower alkyl, or OR′ where R′ is hydrogen, lower alkyl or lower alkanoyl;

A is a bond or a lower alkylene, preferably, C₁-C₄ alkenyl; and

X and X′ are each independently hydrogen, lower alkyl, lower alkoxy, hydroxy, lower alkanoyl, nitro, haloalkyl such as trifluoromethyl, halogen, amino, mono- or di-lower alkyl amino, or when X and X′ are taken together a methylenedioxy group;

R^(c) represents a lower alkyl;

R₂ represents a hydrogen; halogen; substituted or unsubstituted lower alkyl or alkenyl group; lower haloalkyl or haloalkenyl; cyano; acetoamido; lower alkoxy; lower alkylamino; NR^(d)R^(e) where R^(d) and R^(e) are independently hydrogen, lower alkyl, phenyl or phenyl substituted by lower alkyl, lower alkoxy halogen or haloalkyl such as trifluoromethyl or alkoxy; or —SR^(f) where R^(f) is hydrogen, lower alkyl, lower alkanoyl, benzoyl or phenyl;

W represents the group —OCH₂—, —NHCH₂—, —SCH₂— or —NH(C═O)—;

R₃, R₄ and R₅ represent independently a hydrogen, lower alkyl or lower alkenyl, branched or unbranched C₁-C₁₂ alkanoyl, benzoyl or benzoyl substituted by lower alkyl, lower alkoxy, halogen, or R₄ and R₅ form together a five membered ring optionally substituted by a lower alkyl or alkenyl; R₃ further represents independently a phosphate, hydrogen or dihydrogen phosphate, or an alkali metal or ammonium or dialkali or diammonium said thereof;

R₆ represents a hydrogen, halogen atom; or

one of the R groups (i.e. R₁ to R₆) is a sulfohydrocarbon radical of the formula R^(g)—SO₃—R^(h)—, wherein R^(g) represents a group selected from C₁-C₁₀ aliphatic, phenyl and lower alkyl substituted aromatic group which may be substituted or unsubstituted and R^(h) represents a monovalent cation. Suitable monovalent cations include lithium, sodium, potassium, ammonium or trialkyl ammonium, which will enable dissociation to take place under physiological conditions. The remaining R groups being a hydrogen or halogen atom, an unsubstituted hydrocarbon or any other non-sulfur containing group as defined above.

The active ingredient may be as defined above or in the form of salts or solvates thereof, in particular physiologically acceptable salts and solvates thereof. Further, when containing one or more asymmetric carbon atoms, the active ingredient may include isomers and diastereoisomers of the compounds of formula (I) and mixtures thereof.

The hydrocarbon chains used herein may include straight or branched chains. In particular, the terms “alkyl” or “alkenyl” as used herein mean a straight or branched chain alkyl or alkenyl groups.

The terms “lower alkyl or lower alkenyl” mean respectively C₁-C₁₀ alkyl or C₂-C₁₀ alkenyl groups and preferably, C₁-C₆ alkyl and C₂-C₆ alkenyl groups.

Pharmaceutically acceptable salts of the compound of general formula (I) include those derived from pharmaceutically acceptable inorganic and organic acids. Examples of suitable acids include hydrochloric, hydrobromic, sulphoric, nitric, perchloric, fumaric, maleic, phosphoric, glycollic, lactic, salicylic, succinic, toluene-p-sulfonic, tartaric, acetic, citric, methanesulfonic, formic, benzoic, malonic, naphthalene-2-sulfonic and benzenesulfonic acids.

Preferred adenosine derivatives of formula (I) are the N⁶-cyclopentyl adenosine (CPA), 2-chloro-CPA (CCPA), and N⁶-cyclohexyl adenosine (CHA) derivatives, the preparation of which is well known to the person skilled in the art. Other adenosine derivatives which are known to be selective to the A₁ receptor are those wherein R₁ is a anilide group, the latter may be unsubstituted or substituted for example with hydroxyl, alkyl, alkoxy or with a group —CH₂C(O)R″, R″ being an hydroxyl group, —NHCH₃, —NHCH₂CO₂C₂H₅, (ethyl glycinate), tuloidide (also in which the methyl moiety is replaced with a haloalkyl moiety), or with a group —CH₂C(O)NHC₆H₄CH₂C(O)R′″, in which R′″ represents a group to yield a methyl ester substituent (—OCH₃), an amide substituent (e.g. R′″ being a group —NHCH₃), or R′″ being a hydrazide, ethylenediamine, —NHC₂H₅NHC(O)CH₃, 4-(hydroxyphenyl) propionyl, biotinylated ethylene diamine or any other suitable hydrocarbon which renders the compound an A₁ agonist. The preparation of some of the above specific adenosine derivatives is described in the art ⁽⁵⁻⁸⁾

Alternatively, the N⁶-substituted adenosine derivatives used as active ingredients according to the present invention may be those containing an epoxide moiety and more particularly are a cycloalkyl epoxy containing adenosine derivative (e.g. oxabicyclo such as norbornanyl or oxatricyclo such as adamantanyl). Some such compounds may be defined by general formula (I),

wherein R₁ is a group of general formulae (IVa) and (IVb):

wherein M is a Lower alkyl group as defined above.

Embodiments of the agonist compounds having an epoxide N⁶-norbornyl group include the endo and exo isomers and more particularly, can be one of four isomers: the 2R-exo, 2R-endo, 2S-exo and 2S-endo form.

Another embodiment of the N⁶-norbornyl derivative may include an oxygen atom at the N¹-position of the purine ring. This compound is termed N⁶-(5,6-epoxynorborn-2-yl)adenosine-1-oxide.

At times, the active ingredient nay be an adenine derivative in which the β-D-ribofuranozyl moiety of adenosine is replaced with a hydrogen or phenyl group.

The invention has a wide range of therapeutic utilities and provides treatment for a wide range of diseases, disorders or conditions in both human and non-human animals, where induction of proliferation of bone marrow cells may be beneficial to the treated subject. Therapeutic applications include immunomodulation in a subject having a weak immune system, for example: as a result of a genetic disorder; as a result of an infection by an infectious agent, e.g. a virus; as a result of a general stress situation, e.g. following a car or another accident, etc.; as a result of a treatment which causes reduction in the level of leukocytes, particularly neutrophils, e.g. a chemotherapy or treatment with a neuroleptic drug; etc.

A treatment according to the invention may be used to reduce the risk of infection resulting from congenital or acquired neutropenias.

The present invention may also be used for the treatment of subjects having a low count of white blood cells, either a general low count or a count of a specific class of white blood cells, e.g. neutrophils. A weakened immune system manifested by a reduction in white blood cell count is often seen in cancer patients, and when this occurs, this may have a severe effect on the treated patent, and may at times even be a cause of death. In such a case it is thus important to try and increase the white blood cell count. This may be achieved by the treatment in accordance with the invention.

Reduction of white blood cell count, particularly of neutrophils, is very often an undesired side effect of a variety of treatments, including: anti-cancer therapy by chemotherapy or radiotherapy; treatment of a subject with neuroleptic drugs; etc. The active ingredient of the invention may be used in such subject to counter these undesired side effects of the treatment. In accordance with some therapeutic regimes, the active ingredient of the invention may be administered prior to such treatment, or concurrently therewith. For example, in the case of a treatment with a chemotherapeutic drug or treatment with a neuroleptic drug, the active ingredient of the invention may be administered either prior to the onset of treatment with the chemotherapeutic or the neuroleptic drug during such treatment, or may also at times be given after such treatment. In other words, the active ingredient of the invention may be used either as a preventive agent namely to prevent reduction of the white blood cell level as a result of the treatments or may be used as an acute therapeutic agent for simulating an increase in the level of the white blood cells after the level was reduced as a result of said treatment.

In accordance with one embodiment of the invention, an anti-cancer chemotherapeutic agent or a neuroleptic drug may be combined in one formulation with the active ingredient of the invention.

BRIEF DESCRIPTION OF THE FIGURES

In order to understand the invention and to see how it may be carried out in practice, a preferred embodiment will now be described, by way of non-limiting example only, with reference to the accompanying drawings, in which:

FIG. 1 is a bar graph showing results of an in vitro assay in which proliferation of bone marrow cells was tested without adenosine (dense stripes) and with adenosine (spaced stripes) together with adenosine A₁ receptor antagonist (DPCPX) and adenosine A₂ receptor antagonist (DMPX) as compared to a control without any additional added drug. The bar graph shows results of a [³H]thymidine incorporation assay.

FIG. 2 shows [³H]thymidine incorporation assay of a control bone marrow cell preparation (“control”), in the presence of adenosine (“control+adenosine”) and in the presence of two different concentrations of an A₁ receptor agonist, (“CPA”).

DETAILED DESCRIPTION OF A PREFERRED EMBODIMENT

The invention will now be illustrated by the following description of some experiments carried out according thereto.

EXAMPLE 1 In Vitro Evaluation of A₁RAg Materials and Methods Mice

Female ICR or C57BL/6J mice aged 3 months, weighing an average of 25 g were used. The mice were purchased from Harlan Laboratories, Jerusalem, Israel. Standardized pelleted diet and tap water were supplied.

Drugs

All drugs were purchased from Sigma Chemical Co. St. Louis, Mo. Adenosine was dissolved in water and kept as a stock solution in a concentration of 1 mM. For in vitro studies, dilutions in RPMI medium were carried out and final concentrations of 100, 50, 25, 10 and 5 μM were used. For in vivo studies, the stock solution was diluted with PBS to a concentration of 3 mM and 0.5 ml was injected intraperitoneally to mice. 1,3-dipropyl-8-cyclopentylxanthine (DPCPX), an adenosine A₁ receptor antagonist, 3,7-dimethyl-1-propargyl-xanthine (DMPX) an A₂ receptor antagonist and N-cyclopentyladenosine (CPA), a selective A₁ receptor agonist were added to a culture of proliferating bone marrow cells.

Evaluation of Bone Marrow Cell Proliferation in Vitro

Bone marrow cells were obtained from the femur of C57BL/6J mice. Cells were disaggregated by passing through a 25G needle. [³H]-Thymidine incorporation assay was used to evaluate the proliferative capability of the bone marrow cells.

Cells (3×10⁴/well were incubated with RPMI medium, containing 10% fetal calf serum (FCS) (Biological Industries, Beit Haemek, Israel) and adenosine, adenosine antagonists or the agonist in 96 microtiter plates for 48 h. Cultures containing cells were suspended in RPMI medium and 10% FCS served as controls. In the last 6 hours of incubation, each well was pulsed with 1 μCi [³H]-thymidine. Cells were harvested and the ³[H]-thymidine uptake was determined in an LKB liquid scintillation counter (LKB, Piscataway, N.J., USA).

Results Effect of Adenosine, Adenosine Receptor Antagonists and Agonist on Bone Marrow Cell Proliferation

Exposure of bone marrow cells to adenosine at concentrations of 10-50 μM stimulated ³[H]-thymidine incorporation in a concentration dependent manner (Fishman et al.⁽⁴⁾).

To evaluate which adenosine receptor is responsible for this stimulatory effect, two adenosine receptor antagonists were used, i.e., DPCPX (A₁ antagonist) and DMPX (A₂ antagonist). The effect of the antagonists on bone marrow cell proliferation was examined with and without adenosine. In the absence of adenosine, the effect of endogenous adenosine which is released by the bone marrow cells and affects the same cells by a paracrine way, was evaluated. DPCPX (0.1 μM) which block the A₁ receptor, significantly reversed the stimulatory effect of adenosine on bone marrow cell proliferation. DMPX (0.1 μM) given without or with adenosine induced a stimulatory effect on bone marrow cell proliferation (FIG 1). These results show that the A₁ receptor is responsible for the stimulatory effect of adenosine. To confirm this result, CPA, a selective adenosine A₁ receptor agonist was added to a culture of bone marrow cells. CPA induced a statistically significant stimulation of bone marrow cell proliferation at concentrations of 0.1 and 0.01 μM (FIG 2).

EXAMPLE 1 In Vivo Evaluation of A₁RAg Materials And Methods Mice

Male ICR mice of the age of two months and weighing an average of 25 gr were employed. The mice were purchased from Harlan Laboratories, Jerusalem, ISRAEL.

Drug

The cyclopentyl adenosine (CPA), an A₁ adenosine receptor agonist, was used. This drug was purchased Sigma Chemical Co. (St. Louis Mo., USA).

In Vivo Evaluation

Protection of CPA-treated mice against myelotoxic effects of chemotherapy was evaluated. To this end, mice were provided with a chemotherapeutic drug, a combination of the drug with CPA or with a vehicle only. The drug of choice was cyclophosphamide (CPY, given by intraperinoeal injection).

In particular, three test groups of mice were treated daily according to the following regimen:

1. Control group—vehicle only.

2. Chemotherapy—CYP (50 mg/kg body weight).

3. Chemotherapy+chemoprotection—CYP (50 mg/kg body weight)+CPA (6 μg/kg body weight, given through per os administration, 48 h and 72 h following chemotherapy treatment).

To test the myeloprotective effect of CPA, blood samples were withdrawn from the above-mentioned groups 96 h, 120 h and 144 h following treatment with CYP, the following measurements were taken.

Blood cell count-Blood cell count was carried out in a Coulter counter and differential cell counts were performed on smear preparations stained with May-Grunvald-Giemsa solution. Serum was separated from the whole blood and was kept at −70° C.

G-CSF level-granulocyte colony stimulating factor (G-CSF) level in the serum was determined by the use of a commercial ELISA kit (R&D Systems). G-CSF activity was expressed in pgr/ml according to a standard curve of recombinant G-CSF supplied by R&D Systems.

Results

The results obtained show that CPA, an A₁RAg provides in vivo protection against myelotoxicity of chemotherapeutic drugs. Table 1 provides the levels of G-CSF, the number of white blood cells (WBC) and the number of neutrophils form the treated mice, as determined after 96 hours, 120 hours and 144 hours post treatment with the chemotherapeutic drug. Control levels were 6100 WBC and 1200 Neutrophils.

TABLE 1 Neutrophils Treatment G-CSF (pgr/ml) WBC (no.) (no.) CYP (96 hrs) 511.30 2620  377 CYP (96 hrs) + CPA 1508.29 1875  487 CYP (120 hrs) 333.03 2800  490 CYP (120 hrs) + CPA 887.65 4260  494 CYP (144 hrs) 871.14 3900 1326 CYP (144 hrs) + CPA 811.72 5289 2089

These results show that treatment with chemotherapeutic drug only reduce significantly the number of leukocytes and neutrophils white with the combined treatment (CYP+CPA) the level of G-CSF is higher than that obtained with CYP only and the numbers of leukocytes and neutrophils were increased.

Thus, it may be concluded that CPA, given orally to mice, induces in vivo G-CSF production and acts as a chemoprotective agent. 

What is claimed is:
 1. A method for inducing G-CSF secretion within the body of a subject, comprising administering to the subject an effective amount of an agent that is an agonist of the adenosine A₁ receptor for inducing said G-CSF secretion, wherein said agonist of the adenosine A₁ receptor is a compound of general formula (I):

wherein R₁ represents a lower alkyl, substituted or unsubstituted cycloalkyl; a hydroxyl or hydroxyalkyl; a phenyl or lower alkylphenyl, the phenyl or lower alkylphenyl optionally substituted by one or more substituents; —SOR^(c), —SO₂R^(c), —SO₃H, —SO₂NR^(a)R^(b), —OR^(a), —SR^(a), —NHSO₂R^(c), —NHCOR^(a), —NR^(a)R^(b), or —NHR^(a)CO₂R^(b); wherein R^(a) and R^(b) represent independently a hydrogen, lower alkyl, alkanoyl, amino, phenyl or naphthyl, the alkyl group optionally being substituted with a substituted or unsubstituted phenyl or phenoxy group; or when R₁ represents —NR^(a)R^(b), said R^(a) and R^(b) form together with the nitrogen atom a 5- or 6-membered heterocyclic ring optionally containing a second heteroatom selected from the group consisting of oxygen and nitrogen, which second nitrogen heteroatom may optionally be substituted by hydrogen or lower alkyl; or —NR^(a)R^(b) is a group of general formulae (II) or (III):

 wherein n is an integer from 1 to 4; Z is hydrogen, lower alkyl or hydroxyl; Y is hydrogen, lower alkyl, or OR′ where R′ is hydrogen, lower alkyl or lower alkanoyl; A is a bond or a lower alkylene; X and X′ are each independently hydrogen, lower alkyl, lower alkoxy, hydroxy, lower alkanoyl, nitro, haloalkyl, halogen, amino, mono- or di-lower alkyl amino, or when X and X′ are taken together a methylenedioxy group; R^(c) represents a lower alkyl; or R₁ represents an epoxide substituent of general formulae (IVa) or (IVb):

 wherein M is a lower alkylenyl group; R₂ represents hydrogen; halogen; substituted or unsubstituted lower alkyl or alkenyl group; lower haloalkyl or alkenyl; cyano; acetoamido; lower alkoxy; lower alkylamino; NR^(d)R^(e) where R^(d) and R^(e) are independently hydrogen, lower alkyl, phenyl or phenyl substituted by lower alkyl, lower alkoxyl, halogen or haloalkyl; —SR^(f) where R^(f) is hydrogen, lower alkyl, lower alkanoyl, benzoyl or phenyl; W represents —OCH₂—, —NHCH₂—, —SCH₂— or —NH(C═O)—; R_(3,) R₄ and R₅ represent independently a hydrogen, lower alkyl or lower alkenyl, branched or unbranched C₁-C₁₂ alkanoyl, benzoyl or benzoyl substituted by lower alkyl, lower alkoxy or halo group; or R₄ and R₅ form together a 5-membered ring optionally substituted by a lower alkyl or alkenyl; or R₃ further represents independently a phosphate, hydrogenphosphate or dihydrogen phosphate, or an alkali metal or ammonium or dialkali or diammonium salt thereof; R₆ represents a hydrogen or halogen atom; or one of the substituents R₁ to R₆ is a sulfohydrocarbon radical of the formula R^(g)—SO₃—R^(h)—, wherein R^(g) is selected from the group consisting of C₁-C₁₀ alkylenyl, phenylenyl and substituted lower alkyl phenylenyl group and R^(h) represents a monovalent cation; wherein when R₁ is a substituent of general formula (IVb), the N¹ of the compound of general formula (1) may optionally bear an oxygen atom; and pharmaceutically acceptable salts or solvates of said compound.
 2. The method according to claim 1, wherein said subject is a cancer patient.
 3. The method according to claim 2, wherein said subject is a cancer patient whose neutrophil count was reduced as a result of chemotherapy or radiotherapy.
 4. The method according to claim 1, wherein said compound is selected from the group consisting of N⁶-cyclopentyl adenosine (CPA), 2-chloro-CPA (CCPA), and N⁶-cyclohexyl adenosine (CHA).
 5. A method for a therapeutic treatment, comprising administering to a subject in need an effective amount of an agent for achieving a therapeutic effect, the therapeutic effect comprises induction of G-CSF production or secretion, and said agent is an agonist of the adenosine A₁ receptor, wherein said adenosine A₁ receptor agonist is a compound of general formula (I):

wherein R₁ represents a lower alkyl, substituted or unsubstituted cycloalkyl; a hydroxyl or hydroxyalkyl; a phenyl or lower alkylphenyl, the phenyl and lower alkylphenyl are optionally substituted by one or more substituents; —SOR^(c), —SO₂R^(c), —SO₃H, —SO₂NR^(a)R^(b), —OR^(a), —SR^(a), —NHSO₂R^(c), —NHCOR^(a), —NR^(a)R^(b), or —NHR^(a)CO₂R^(b); wherein R³ and R^(b) represent independently a hydrogen, lower alkyl, alkanoyl, amino, phenyl or naphthyl, the alkyl group optionally being substituted with a substituted or unsubstituted phenyl or phenoxy group; or when R₁ represents —NR^(a)R^(b), said R^(a) and R^(b) form together with the nitrogen atom a 5- or 6-membered heterocyclic ring optionally containing a second heteroatom selected from the group consisting of oxygen and nitrogen, which second nitrogen heteroatom may optionally be further substituted by hydrogen or lower alkyl; or —NR^(a)R^(b) is a group of general formulae (II) or (III):

 wherein n is an integer from 1 to 4; Z is hydrogen, lower alkyl or hydroxyl; Y is hydrogen, lower alkyl, or OR′ where R′ is hydrogen, lower alkyl or lower alkanoyl; A is a bond, a lower alkylene, or a C₁-C₄ alkenyl; X and X′ are each independently hydrogen, lower alkyl, lower alkoxy, hydroxy, lower alkanoyl, nitro, haloalkyl, halogen, amino, mono- or di-lower alkyl amino, or when X and X′ are taken together a methylenedioxy group; R^(c) represents a lower alkyl; or R₁ represents an epoxide substituent of general formulae (IVa) or (IVb):

 wherein M is a lower alkylenyl group; R₂ represents hydrogen; halogen; substituted or unsubstituted lower alkyl or alkenyl group; lower haloalkyl or alkenyl; cyano; acetoamido; lower alkoxy; lower alkylamino; NR^(d)R^(e) where R^(d) and R^(e) are independently hydrogen, lower alkyl, phenyl or phenyl substituted by lower alkyl, lower alkoxy, halogen or haloalkyl or alkoxyl; —SR^(f) where R^(f) is hydrogen, lower alkyl, lower alkanoyl, benzoyl or phenyl; W represents —OCH₂—, —NHCH₂—, —SCH₂— or —NH(C═O)—; R_(3,) R₄ and R₅ represent independently a hydrogen, lower alkyl or lower alkenyl, branched or unbranched C₁-C₁₂ alkanoyl, benzoyl or benzoyl substituted by lower alkyl, lower alkoxy or halo group; or R₄ and R₅ form together a 5-membered ring optionally substituted by a lower alkyl or alkenyl; R₃ further represents independently a phosphate, hydrogen phosphate or dihydrogen phosphate, or an alkali metal or ammonium or dialkali or diammonium salt thereof; R₆ represents a hydrogen or halogen atom; or one of the substituents R₁ to R₆ is a sulfohydrocarbon radical of the formula R^(g)—SO₃—R^(h)—, wherein R^(g) is selected from the group consisting of C₁-C₁₀alkylenyl, phenylenyl and substituted lower alkyl phenylenyl group and R^(h) represents a monovalent cation; wherein when R₁ is a substituent of general formula (IVb), the N¹-position of the compound of general formula (1) may optionally bear an oxygen atom; and pharmaceutically acceptable salts or solvates of said compound.
 6. The method according to claim 5, wherein said therapeutic effect is to counter drug-induced myelotoxicity.
 7. The method according to claim 5, wherein said drug is a chemotherapeutic drug given to the subject within the framework of anti-cancer treatment.
 8. The method according to claim 6, wherein said compound is selected from N⁶-cyclopentyl adenosine (CPA), 2-chloro-CPA (CCPA), and N⁶-cyclohexyl adenosine (CHA).
 9. The method according to claim 1, wherein A is C₁-C₄ alkenyl, or X or X′ is trifluoromethyl.
 10. The method according to claim 5, wherein X or X′ is trifluoromethyl.
 11. The method according to claim 1, wherein X or X′ are independently trifluoromethyl. 